JT780 - SR INSTRUMENT TECHNICIAN

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:
• Provides advanced instrumentation and process control support for manufacturing and utility systems and analytical laboratory equipment
• Responsible for calibration, installation, troubleshooting, loop checking, programming, repair, validation support, and technical documentation of instrumentation and process control systems
• Perform advanced calibration, troubleshooting, repair, installation, and maintenance of instrumentation used on manufacturing and utility equipment
• Perform loop checks, loop tuning, and troubleshooting of process control systems
• Design, install, configure, and start up instruments and microprocessor-based controllers used for process control
• Troubleshoot and repair hardware and software issues associated with computer-based process control systems
• Perform advanced programming and troubleshooting of PLC, DCS, BMS, and MMI systems
• Support start-up and commissioning of new equipment to ensure instrumentation meets established design specifications
• Evaluate existing calibration cycles and recommend changes to optimize equipment reliability and the calibration program
• Maintain accurate calibration records, instrument files, work orders, and technical documentation
• Maintain and manage an up-to-date spare parts inventory for instrumentation and process control equipment
• Perform equipment certification activities to verify compliance with applicable industry standards and client procedures
• Assist with the development and execution of validation documentation for instrumentation and control systems
• Develop, revise, review, and maintain SOPs and technical procedures related to instrumentation and process control activities
• Maintain and update loop sheets, electrical schematics, P&IDs, I/O wiring documentation, and panel drawings
• Support manufacturing and utility operations by planning and coordinating instrumentation activities to minimize impact to production
• Coordinate work performed by personnel and contractors with Operations and other site stakeholders
• Develop and maintain technical training programs to strengthen team knowledge of instrumentation, controls, and plant systems
• Maintain required cGMP training documentation and ensure training requirements remain current
• Support investigations, troubleshooting activities, equipment modifications, and process improvements related to instrumentation and control systems
• Ensure all activities are performed in accordance with CFRs, cGMP requirements, SOPs, safety requirements, and client policies
• Provide technical guidance and support to other members of the instrumentation and controls team
• May assume lead responsibilities within the work team and provide direction to technicians or contractors

Qualifications:
• Associate’s degree in instrumentation or related area.
• 1 + year of instrumentation experience. Preferred in regulated environments.
• GxP Documentation
• Basic Calibration of Temperature, Pressure, Level and Analytical Instrumentation
• Sanitary Diaphragms and Gaskets replacement skills
• Autoclave/Glasswasher skills
• Maximo CMMS Documentation
• Technical Documentation skills
• Lock Out/Tag Out (LOTO) skills
• Advanced hands-on knowledge of pneumatic, mechanical, electronic, and process instrumentation
• Strong understanding of process control loops, loop checks, and loop tuning
• Experience programming and troubleshooting computer-based control systems
• Hands-on experience with PLC, DCS, BMS, and MMI systems
• Knowledge of analog and digital electronics, microprocessors, computers, and field instrumentation
• Experience with calibration, installation, troubleshooting, repair, and maintenance of instrumentation and control systems
• Ability to interpret and update P&IDs, loop sheets, electrical schematics, I/O wiring, and panel drawings
• Experience supporting equipment start-up, commissioning, validation, or qualification activities
• Knowledge of cGMP, CFRs, SOPs, and regulated pharmaceutical/biotech manufacturing environments
• Ability to support on-call activities when required
• Non-Standard Shift. Must be available for multiple shifts
• Shift: 5:00am – 5:00pm (12 hours)